Canonical Allele Identifier: CA519706210

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581469C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353101C>G , CM000685.2:g.154353101C>G	GRCh38
NC_000023.10:g.153581469C>G , CM000685.1:g.153581469C>G	GRCh37
NC_000023.9:g.153234663C>G	NCBI36
NG_011506.1:g.26538G>C
NG_011506.2:g.26538G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6102G>C	ENSP00000353467.4:p.Ser2034=
ENST00000369850.10:c.6126G>C MANE Select	ENSP00000358866.3:p.Ser2042=
ENST00000369856.8:c.6045G>C	ENSP00000358872.4:p.Ser2015=
ENST00000422373.6:c.3161-426G>C	ENSP00000416926.2:n.3161-426G>C
ENST00000610817.5:c.6183G>C	ENSP00000480593.2:n.6183G>C
ENST00000673639.2:c.280-4411G>C
ENST00000676696.1:c.6405G>C	ENSP00000503392.1:n.6405G>C
ENST00000678304.1:n.1305G>C
ENST00000344736.8:c.6006G>C	ENSP00000358863.3:p.Ser2002=
ENST00000360319.8:c.6102G>C	ENSP00000353467.4:p.Ser2034=
ENST00000369850.7:c.6126G>C	ENSP00000358866.3:p.Ser2042=
ENST00000369856.7:c.6045G>C	ENSP00000358872.4:p.Ser2015=
ENST00000415241.1:c.328G>C
ENST00000420627.5:c.6082G>C	ENSP00000408921.1:n.6082G>C
ENST00000422373.5:c.6102G>C	ENSP00000416926.1:p.Ser2034=
ENST00000444578.1:c.69G>C	ENSP00000397824.1:p.Ser23=
ENST00000466325.1:n.265G>C
ENST00000490936.5:n.2115G>C
ENST00000610817.4:c.5844+292G>C	ENSP00000480593.1:n.5844+292G>C
NM_001110556.1:c.6126G>C	NP_001104026.1:p.Ser2042=
NM_001456.3:c.6102G>C	NP_001447.2:p.Ser2034=
XM_011531127.1:c.6030G>C	XP_011529429.1:p.Ser2010=
XM_011531128.1:c.6006G>C	XP_011529430.1:p.Ser2002=
XM_011531129.1:c.5952G>C	XP_011529431.1:p.Ser1984=
XM_011531130.1:c.5928G>C	XP_011529432.1:p.Ser1976=
XM_011531131.1:c.5925G>C	XP_011529433.1:p.Ser1975=
NM_001110556.2:c.6126G>C MANE Select	NP_001104026.1:p.Ser2042=
NM_001456.4:c.6102G>C	NP_001447.2:p.Ser2034=